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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840176Generated: October 30, 2026

Methyl iodide → HCID 23506070, compound

https://huagongshe.com/reaction/1840176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
Reactant3-[[3-[(4-Methoxyphenyl)amino]phenyl]-[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanolHCID 23506028—
ReactantHCID 131724296HCID 131724296—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23506070HCID 23506070—

Reaction Conditions

Temperature23 °C

Reaction Steps

To a solution of 3-[[3-[(4methoxyphenyl)amino]phenyl]-[[3-(1,1,2,2-tetrafluoro-ethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanol (44.3 mg, 0.083 mmol) in tetrahydrofuran (1.0 mL), methyl iodide (6.21 μL, 0.099 mmol) and cesium carbonate (36.6 mg, 0.112 mmol) were added. The dark solution was stirred at 23° C. for 2 h, then heated to 55° C. for 12 h. The reaction mixture was filtered through celite, and the residue was purified by silica gel chromatography eluting with 20% ethyl acetate in hexane to give 25.2 mg (55%) of the desired 3-[[3-[(4methoxyphenyl)methylamino]-phenyl][[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methylamino]-1,1,1-trifluoro-2-propanol product as an orange oil. HRMS calcd for C26H25F7N2O3: 546.1753, found: 546.1750 [M]+. 1H NMR (CDCl3), δ 3.54 (m, 1H), 3.38 (s, 3H), 3.65-3.80 (m, 4H), 4.59 (s, 2H), 5.90 (tt, 1H), 6.20 (d, 1H), 6.37 (d, 1H), 6.68 (s, 1H), 6.76 (d, 2H), 6.90-7.15 (m, 6H), 7.31 (t, 1H). 19F NMR (CDCl3), δ −137.21 (d, 2F), −88.52 (s, 2F), −78.79 (s, 3F).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677379B2
Source datasetuspto-grants-2004_01
ORD IDord-f5de2de7f3444dedbb3ac373b751f1d6
Source noteuspto-grants-2004_01